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Article

Lack of pancreatic body and tail in HNF1B mutation carriers.

Diabetic medicine : a journal of the British Diabetic Association - 1 Jul 2008

Haldorsen I S, Vesterhus M, Raeder H, Jensen D K, Søvik O, Molven A, Njølstad P R

Abstract excerpt

AIMS: Hepatocyte nuclear factor 1B (HNF1B) gene mutation carriers have a systemic disease characterized by congenital malformations in the urogenital tract, diabetes mellitus of maturity-onset diabetes of the young type and dysfunction of the liver and exocrine pancreas. We aimed to investigate p...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18644064
DOI: 10.1111/j.1464-5491.2008.02460.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18644064-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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